FDA UDI In Commercial Distribution 🇺🇸 United States

Kestra Provided Device Patient Application

DI: 00840241600399 · Model: 80740-005 · Kestra Medical Technologies, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kestra Provided Device Patient Application
Primary DI
00840241600399
Version / Model
80740-005
Catalog Number
80740-005
Company Name
Kestra Medical Technologies, Inc.
Labeler DUNS
060944361
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-04-30
Public Version
1
Public Version Date
2025-05-08
Public Version Status
New
Public Device Record Key
01f721c9-8dba-4235-8de1-570d9bd22914

Device Description

ASSURE Patient Application for the Kestra Provided Device.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OUG Medical Device Data System

GMDN Terms

Code Name
57967 Medical equipment clinical data interfacing software

Identifiers

Type ID
Primary 00840241600399